Motwani, Jayashree
19  results:
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9

Rivaroxaban compared with standard anticoagulants for the t..:

Male, Christoph ; Lensing, Anthonie ; Palumbo, Joseph...
info:eu-repo/semantics/altIdentifier/doi/10.1016/S2352-3026(19)30219-4.  , 2019
 
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10

Rivaroxaban compared with standard anticoagulants for the t..:

Male, Christoph ; Lensing, Anthonie ; Palumbo, Joseph...
info:eu-repo/semantics/altIdentifier/doi/10.1016/S2352-3026(19)30219-4.  , 2019
 
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11

Rivaroxaban compared with standard anticoagulants for the t..:

Male, Christoph ; Lensing, Anthonie ; Palumbo, Joseph...
info:eu-repo/semantics/altIdentifier/doi/10.1016/S2352-3026(19)30219-4.  , 2019
 
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13

Whole exome sequencing identifies genetic variants in inher..:

Johnson, Ben ; Lowe, Gillian C ; Futterer, Jane...
Johnson , B , Lowe , G C , Futterer , J , Lordkipanidzé , M , Macdonald , D , Simpson , M A , Sanchez-Guiú , I , Drake , S , Bem , D , Leo , V , Fletcher , S J , Dawood , B , Rivera , J , Allsup , D , Biss , T , Bolton-Maggs , P H , Collins , P , Curry , N , Grimley , C , James , B , Makris , M , Motwani , J , Pavord , S , Talks , K , Thachil , J , Wilde , J , Williams , M , Harrison , P , Gissen , P , Mundell , S , Mumford , A , Daly , M E , Watson , S P & Morgan , N V 2016 , ' Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects ' , Haematologica , vol. 101 , no. 10 , pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316.  , 2016
 
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15

Whole Exome Sequencing Identifies Genetic Variants In Inher..:

Johnson, Ben ; Lowe, Gillian C ; Futterer, Jane...
Johnson , B , Lowe , G C , Futterer , J , Lordkipanidze' , M , MacDonald , D , Simpson , M A , Sanchez Guiu' , I , Drake , S , Bem , D , Leo , V , Fletcher , S J , Dawood , B , Rivera , J , Allsup , D , Biss , T , Bolton-Maggs , P H B , Collins , P , Curry , N , Grimley , C , James , B , Makris , M , Motwani , J , Pavord , S , Talks , K , Thachil , J , Wilde , J , Williams , M , Harrison , P , Gissen , P , Mundell , S J , Mumford , A , Daly , M E , Watson , S P , Morgan , N V 2016 , ' Whole Exome Sequencing Identifies Genetic Variants In Inherited Thrombocytopenia With Secondary Qualitative Function Defects ' , Haematologica , vol. 101 , no. 10 , pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316.  , 2016
 
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